6-Formyl-7-hydroxy-5-methoxy-4-methylphthalide

Details

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Internal ID 5f036033-71dc-4edd-b5f9-186189e18672
Taxonomy Organoheterocyclic compounds > Isocoumarans > Isobenzofuranones > Phthalides
IUPAC Name 4-hydroxy-6-methoxy-7-methyl-3-oxo-1H-2-benzofuran-5-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H10O5/c1-5-7-4-16-11(14)8(7)9(13)6(3-12)10(5)15-2/h3,13H,4H2,1-2H3
InChI Key AMMRYTGRYFXAEQ-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C11H10O5
Molecular Weight 222.19 g/mol
Exact Mass 222.05282342 g/mol
Topological Polar Surface Area (TPSA) 72.80 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.19
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-Formyl-7-hydroxy-5-methoxy-4-methylphthalide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9848 98.48%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6998 69.98%
OATP2B1 inhibitior - 0.8574 85.74%
OATP1B1 inhibitior + 0.9058 90.58%
OATP1B3 inhibitior + 0.9631 96.31%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9303 93.03%
P-glycoprotein inhibitior - 0.9565 95.65%
P-glycoprotein substrate - 0.9566 95.66%
CYP3A4 substrate - 0.5127 51.27%
CYP2C9 substrate - 0.5744 57.44%
CYP2D6 substrate - 0.8506 85.06%
CYP3A4 inhibition - 0.8802 88.02%
CYP2C9 inhibition + 0.6784 67.84%
CYP2C19 inhibition - 0.7385 73.85%
CYP2D6 inhibition - 0.9101 91.01%
CYP1A2 inhibition + 0.6669 66.69%
CYP2C8 inhibition - 0.8324 83.24%
CYP inhibitory promiscuity - 0.7548 75.48%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.6420 64.20%
Eye corrosion - 0.9576 95.76%
Eye irritation + 0.9680 96.80%
Skin irritation - 0.7197 71.97%
Skin corrosion - 0.9507 95.07%
Ames mutagenesis + 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7938 79.38%
Micronuclear - 0.5126 51.26%
Hepatotoxicity + 0.8250 82.50%
skin sensitisation - 0.8123 81.23%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.5965 59.65%
Acute Oral Toxicity (c) II 0.4700 47.00%
Estrogen receptor binding - 0.5563 55.63%
Androgen receptor binding - 0.5610 56.10%
Thyroid receptor binding - 0.7878 78.78%
Glucocorticoid receptor binding - 0.5813 58.13%
Aromatase binding - 0.6036 60.36%
PPAR gamma + 0.5521 55.21%
Honey bee toxicity - 0.9428 94.28%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.9570 95.70%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL2002 P12268 Inosine-5'-monophosphate dehydrogenase 2 98.90% 98.21%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.83% 95.56%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 97.51% 98.11%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.70% 91.11%
CHEMBL2581 P07339 Cathepsin D 87.93% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.68% 99.23%
CHEMBL1951 P21397 Monoamine oxidase A 87.41% 91.49%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.09% 94.45%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 85.22% 93.40%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.58% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.92% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.89% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 81.35% 94.73%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Hymenaea oblongifolia

Cross-Links

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PubChem 21861510
LOTUS LTS0233370
wikiData Q104914738